HomeChinaFoosin Medical Supplies Inc., Ltd.

Foosin Medical Supplies Inc., Ltd.

China · Weihai Shandong
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Singapore, South Korea, Israel, Russia — 6 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
8listed device types
Class I 0Class II 8Class III 0
plus 10 registration records and 10 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
2 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
2device registrations
CLASS D 2
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
2active registrations
Class 2b 1Class 3 1
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States10 registration records, 10 510(k), 0 PMA
Manufacturer names merged into this page: FOOSIN MEDICAL SUPPLIES INC.LTD · FOOSIN MEDICAL SUPPLIES INC., LTD.

Company information

Country
China
City
Weihai Shandong

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

22008
32014 · K142810
12017 · K170842
22019 · K183004
22020 · K201139

FDA listed device types

Suture, Surgical, Absorbable, Polydioxanone 1Suture, Nonabsorbable, Silk 1Suture, Nonabsorbable, Synthetic, Polypropylene 1Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene 1Suture, Nonabsorbable, Synthetic, Polyethylene 1Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile 1Suture, Absorbable, Synthetic, Polyglycolic Acid 1Suture, Nonabsorbable, Synthetic, Polyamide 1

Registration details (sample)

MarketIdentifierNameClass / date
USK201139WEGO-PDO Barbed Suture2020-10-20
USK193209Wego-Stainless Steel2020-02-19
USK183004WEGO-PGA RAPID2019-01-28

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